Literature DB >> 11489209

The unfolded protein response: no longer just a special teams player.

E Spear1, D T Ng.   

Abstract

The endoplasmic reticulum stress pathway known as the unfolded protein response is currently the best understood model of interorganellar signal transduction. Bridging a physical separation, the pathway provides a direct line of communication between the endoplasmic reticulum lumen and the nucleus. With the unfolded protein response, the cell has the means to monitor and respond to the changing needs of the endoplasmic reticulum. Beginning with the discovery of its remarkable signaling mechanism in yeast, the unfolded protein response has not ceased to reveal more of its many secrets. By applying powerful biochemical, genetic, genomic, and cytological approaches, the recent efforts of many groups have buried the long-held notion that the unfolded protein response is simply a regulatory platform for endoplasmic reticulum chaperones. We now know that the unfolded protein response regulates many genes that affect diverse aspects of cellular physiology. In addition, studies in mammals have revealed novel unfolded protein response signaling factors that may contribute to the specialized needs of multicellular organisms. This article focuses on these and other recent developments in the field.

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Year:  2001        PMID: 11489209     DOI: 10.1034/j.1600-0854.2001.20801.x

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


  23 in total

1.  A mitochondrial specific stress response in mammalian cells.

Authors:  Quan Zhao; Jianghui Wang; Ilya V Levichkin; Stan Stasinopoulos; Michael T Ryan; Nicholas J Hoogenraad
Journal:  EMBO J       Date:  2002-09-02       Impact factor: 11.598

2.  Stress tolerance of misfolded carboxypeptidase Y requires maintenance of protein trafficking and degradative pathways.

Authors:  Eric D Spear; Davis T W Ng
Journal:  Mol Biol Cell       Date:  2003-03-20       Impact factor: 4.138

3.  Substrate recognition in ER-associated degradation mediated by Eps1, a member of the protein disulfide isomerase family.

Authors:  Qiongqing Wang; Amy Chang
Journal:  EMBO J       Date:  2003-08-01       Impact factor: 11.598

4.  The unfolded protein response regulates glutamate receptor export from the endoplasmic reticulum.

Authors:  Jaegal Shim; Tohru Umemura; Erika Nothstein; Christopher Rongo
Journal:  Mol Biol Cell       Date:  2004-08-18       Impact factor: 4.138

5.  The protein translocation channel binds proteasomes to the endoplasmic reticulum membrane.

Authors:  Kai-Uwe Kalies; Susanne Allan; Tatiana Sergeyenko; Heike Kröger; Karin Römisch
Journal:  EMBO J       Date:  2005-06-23       Impact factor: 11.598

Review 6.  The protective and destructive roles played by molecular chaperones during ERAD (endoplasmic-reticulum-associated degradation).

Authors:  Jeffrey L Brodsky
Journal:  Biochem J       Date:  2007-06-15       Impact factor: 3.857

7.  Pbn1p: an essential endoplasmic reticulum membrane protein required for protein processing in the endoplasmic reticulum of budding yeast.

Authors:  Shoba Subramanian; Carol A Woolford; Emily Drill; Meng Lu; Elizabeth W Jones
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-17       Impact factor: 11.205

Review 8.  Mitochondrial stress: a bridge between mitochondrial dysfunction and metabolic diseases?

Authors:  Fang Hu; Feng Liu
Journal:  Cell Signal       Date:  2011-05-15       Impact factor: 4.315

9.  Rapamycin inhibits postprandial-mediated X-box-binding protein-1 splicing in rat liver.

Authors:  Kyle T Pfaffenbach; Angela M Nivala; Lauren Reese; Flannery Ellis; Dong Wang; Yuren Wei; Michael J Pagliassotti
Journal:  J Nutr       Date:  2010-03-17       Impact factor: 4.798

10.  The cell wall and endoplasmic reticulum stress responses are coordinately regulated in Saccharomyces cerevisiae.

Authors:  Damian J Krysan
Journal:  Commun Integr Biol       Date:  2009-05
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